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Large-scale production of recombinant miraculin protein in transgenic carrot callus suspension cultures using air-lift bioreactors

Miraculin, derived from the miracle fruit (Synsepalum dulcificum), is a taste-regulating protein that interacts with human sweet-taste receptors and transforms sourness into sweet taste. Since miracle fruit is cultivated in West Africa, mass production of miraculin is limited by regional and seasona...

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Autores principales: Park, Yun-Ji, Han, Jong-Eun, Lee, Hyoshin, Jung, Yu-Jin, Murthy, Hosakatte Niranjana, Park, So-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426344/
https://www.ncbi.nlm.nih.gov/pubmed/32789704
http://dx.doi.org/10.1186/s13568-020-01079-3
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author Park, Yun-Ji
Han, Jong-Eun
Lee, Hyoshin
Jung, Yu-Jin
Murthy, Hosakatte Niranjana
Park, So-Young
author_facet Park, Yun-Ji
Han, Jong-Eun
Lee, Hyoshin
Jung, Yu-Jin
Murthy, Hosakatte Niranjana
Park, So-Young
author_sort Park, Yun-Ji
collection PubMed
description Miraculin, derived from the miracle fruit (Synsepalum dulcificum), is a taste-regulating protein that interacts with human sweet-taste receptors and transforms sourness into sweet taste. Since miracle fruit is cultivated in West Africa, mass production of miraculin is limited by regional and seasonal constraints. Here, we investigated mass production of recombinant miraculin in carrot (Daucus carota L.) callus cultures using an air-lift bioreactor. To increase miraculin expression, the oxidative stress-inducible SWPA2 promoter was used to drive the expression of miraculin gene under various stress treatments. An 8 h treatment of hydrogen peroxide (H(2)O(2)) and salt (NaCl) increased the expression of miraculin gene by fivefold compared with the untreated control. On the other hand, abscisic acid, salicylic acid, and methyl jasmonate treatments showed no significant impact on miraculin gene expression compared with the control. This shows that since H(2)O(2) and NaCl treatments induce oxidative stress, they activate the SWPA2 promoter and consequently up-regulate miraculin gene expression. Thus, the results of this study provide a foundation for industrial-scale production of recombinant miraculin protein using transgenic carrot cells as a heterologous host.
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spelling pubmed-74263442020-08-19 Large-scale production of recombinant miraculin protein in transgenic carrot callus suspension cultures using air-lift bioreactors Park, Yun-Ji Han, Jong-Eun Lee, Hyoshin Jung, Yu-Jin Murthy, Hosakatte Niranjana Park, So-Young AMB Express Original Article Miraculin, derived from the miracle fruit (Synsepalum dulcificum), is a taste-regulating protein that interacts with human sweet-taste receptors and transforms sourness into sweet taste. Since miracle fruit is cultivated in West Africa, mass production of miraculin is limited by regional and seasonal constraints. Here, we investigated mass production of recombinant miraculin in carrot (Daucus carota L.) callus cultures using an air-lift bioreactor. To increase miraculin expression, the oxidative stress-inducible SWPA2 promoter was used to drive the expression of miraculin gene under various stress treatments. An 8 h treatment of hydrogen peroxide (H(2)O(2)) and salt (NaCl) increased the expression of miraculin gene by fivefold compared with the untreated control. On the other hand, abscisic acid, salicylic acid, and methyl jasmonate treatments showed no significant impact on miraculin gene expression compared with the control. This shows that since H(2)O(2) and NaCl treatments induce oxidative stress, they activate the SWPA2 promoter and consequently up-regulate miraculin gene expression. Thus, the results of this study provide a foundation for industrial-scale production of recombinant miraculin protein using transgenic carrot cells as a heterologous host. Springer Berlin Heidelberg 2020-08-13 /pmc/articles/PMC7426344/ /pubmed/32789704 http://dx.doi.org/10.1186/s13568-020-01079-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Park, Yun-Ji
Han, Jong-Eun
Lee, Hyoshin
Jung, Yu-Jin
Murthy, Hosakatte Niranjana
Park, So-Young
Large-scale production of recombinant miraculin protein in transgenic carrot callus suspension cultures using air-lift bioreactors
title Large-scale production of recombinant miraculin protein in transgenic carrot callus suspension cultures using air-lift bioreactors
title_full Large-scale production of recombinant miraculin protein in transgenic carrot callus suspension cultures using air-lift bioreactors
title_fullStr Large-scale production of recombinant miraculin protein in transgenic carrot callus suspension cultures using air-lift bioreactors
title_full_unstemmed Large-scale production of recombinant miraculin protein in transgenic carrot callus suspension cultures using air-lift bioreactors
title_short Large-scale production of recombinant miraculin protein in transgenic carrot callus suspension cultures using air-lift bioreactors
title_sort large-scale production of recombinant miraculin protein in transgenic carrot callus suspension cultures using air-lift bioreactors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426344/
https://www.ncbi.nlm.nih.gov/pubmed/32789704
http://dx.doi.org/10.1186/s13568-020-01079-3
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